Job Description
Overview
- $26/hr - $34/hr (depending on experience)
- Great benefits including 401k w/match and 15 days PTO
- Monday-Friday, 8:30 AM - 5 PM
- Coordinators typically see 3–5 patients daily, with higher volumes during high-enrollment studies.
About Our Client
Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors.
Responsibilities
- Obtaining informed consent per ICH/GCP and site SOPs.
- Reviewing and revising source documents and interviewing and collecting data from study participants.
- Participating in protocol training meetings and completing online training for protocol-specific software programs.
- Dispensing/collecting study medication and providing accurate Investigational Product accountability.
- Working with our lab specialist to obtain study participant laboratory specimens according to protocol
- Completing study participant tracking information (either electronic or manual) accurately and on a timely basis. Responding and resolving data queries in a prompt manner.
- Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol.
- Performing basic data manipulation.
- Maintaining a thorough understanding of all assigned clinical trial protocols.
- Other duties as assigned
Qualifications:
- 1+ years of experience as a CRC with a research site
- Bachelor's degree preferred
- Phlebotomy and EKG experience preferred
- Familiar with e-source reporting via an electronic platform